Biomass Or Glycerol to Biofuels

Total Page:16

File Type:pdf, Size:1020Kb

Biomass Or Glycerol to Biofuels University of Pennsylvania ScholarlyCommons Department of Chemical & Biomolecular Senior Design Reports (CBE) Engineering 4-2010 BIOMASS OR GLYCEROL TO BIOFUELS Jeanne Ho University of Pennsylvania Joseph Luchtan University of Pennsylvania Andrew Perlman University of Pennsylvania Andrew Solute University of Pennsylvania Follow this and additional works at: https://repository.upenn.edu/cbe_sdr Part of the Biochemical and Biomolecular Engineering Commons Ho, Jeanne; Luchtan, Joseph; Perlman, Andrew; and Solute, Andrew, "BIOMASS OR GLYCEROL TO BIOFUELS" (2010). Senior Design Reports (CBE). 13. https://repository.upenn.edu/cbe_sdr/13 This paper is posted at ScholarlyCommons. https://repository.upenn.edu/cbe_sdr/13 For more information, please contact [email protected]. BIOMASS OR GLYCEROL TO BIOFUELS Abstract In the past decade, many advances were made towards the production of alternative fuels. Biodiesel is one such alternative fuel which has received much attention and research. However, its production also creates an abundance of crude glycerol, which is a waste product that has little value and is costly to purify. Therefore, a process which can utilize crude glycerol deserves analysis. In our project, a process was designed for the manufacture of various high value products from glycerol. This process used catalyst technology and reaction data from Virent Energy Systems, Inc. to convert crude glycerol feed into the products of hexane, butane, ethane, propane, and hydrogen. Our proposed process design yields a NPV of $238,317,900.00 and an IRR of 8.18%. Disciplines Biochemical and Biomolecular Engineering This working paper is available at ScholarlyCommons: https://repository.upenn.edu/cbe_sdr/13 Department of Chemical & Biomolecular Engineering Senior Design Report (CBE) University of Pennsylvania Year 2010 Biomass or Glycerol to Biofuels Jeanne Ho, Joseph Luchtan, Andrew Perlman, and Andrew Salute University of Pennsylvania Biomass or Glycerol to Biofuels Written by: Jeanne Ho Joseph Luchtan Andrew Perlman Andrew Salute Industrial Consultant: Mr. Stephen M. Tieri Faculty Advisor: Dr. John Vohs April 13, 2010 University of Pennsylvania Department of Chemical & Biomolecular Engineering University of Pennsylvania School of Engineering and Applied Science Department of Chemical and Biomolecular Engineering 220 South 33rd Street Philadelphia, PA 19104 April 13, 2010 Dear Mr. Fabiano, Dr. Vohs, and Stephen Tieri Enclosed is our proposed process design for the Biomass or Glycerol to Biofuels problem statement provided by Stephen M. Tieri of DuPont. Our solution includes four main parts: selection of raw materials, pretreatment, reactions, and separations. This process achieves the required 1MM gallons of product capacity specified by the problem statement. The following report details the process, the equipment needs and estimated costs, the utility requirements, and a detailed economic analysis. Our proposed process design yields a NPV of $238,317,900.00 and an IRR of 8.18%. Detailed economic analyses, including sensitivities to key input assumptions, have also been included and discussed. Feed and product costs and other potential risks to the long-term profitability of the process have also been addressed. Sincerely, Jeanne Ho Joseph Luchtan Andrew Perlman Andrew Salute Contents Abstract..........................................................................................................................7 Project Charter................................................................................................................9 Introduction..................................................................................................................12 Market Analysis............................................................................................................18 Pre-treatment.................................................................................................................22 Introduction...............................................................................................................23 Process Inputs............................................................................................................23 Pretreatment..............................................................................................................26 Comparison...............................................................................................................28 Process Background......................................................................................................30 Reactions...................................................................................................................31 Separations................................................................................................................35 Process Flow Diagram and Material Balance.................................................................39 Section 100: Reaction Train..........................................................................................50 Detailed Unit Descriptions.........................................................................................52 Section 200: Separations of CO2 and H2 ........................................................................57 Detailed Unit Descriptions.......................................................................................59 Sections 300 and 400: Tower Separations and Purification of Products...................62 Detailed Unit Descriptions.......................................................................................63 Section 500: Recycle Process ......................................................................................65 Detailed Unit Descriptions.......................................................................................67 Considerations for ASPEN Design................................................................................69 Aqueous Phase Reforming.........................................................................................70 Base-Catalyzed Condensation and Hydrodeoxygenation............................................76 CO2 Scrubbing with MEA.........................................................................................81 H2 Removal by PRISM Membrane............................................................................81 Difficulties Encountered in Separation Processes..........................................................82 Unit Specifications........................................................................................................85 Equipment Cost Summary...........................................................................................113 Energy Requirements..................................................................................................117 Utilities....................................................................................................................118 Heat Exchangers......................................................................................................122 Financial Analysis.......................................................................................................126 Introduction.............................................................................................................127 General Information................................................................................................129 Product Information.................................................................................................137 Chronology..............................................................................................................137 Equipment Costs......................................................................................................138 Raw Materials.........................................................................................................140 Byproducts..............................................................................................................140 Utilities....................................................................................................................140 Variable Costs.........................................................................................................141 Working Capital......................................................................................................141 Total Permanent Investment....................................................................................142 Fixed Costs..............................................................................................................142 Cost Summary.........................................................................................................144 Variable Costs and Fixed Costs...............................................................................148 Investment Summary and Working Capital..............................................................149 Cash Flows and Profitability Measures....................................................................150 Sensitivity Analyses....................................................................................................153 Variable Costs.........................................................................................................153 Product Price...........................................................................................................153 Inflation...................................................................................................................154
Recommended publications
  • (12) United States Patent (10) Patent No.: US 7.494,962 B2 Kinet Al
    USOO74949.62B2 (12) United States Patent (10) Patent No.: US 7.494,962 B2 Kinet al. (45) Date of Patent: Feb. 24, 2009 (54) SOLVENTS CONTAINING CYCLOAKYL (56) References Cited ALKYLETHERS AND PROCESS FOR PRODUCTION OF THE ETHERS U.S. PATENT DOCUMENTS 3496,223 A * 2/1970 Mitchell et al. ............... 562/22 (75) Inventors: Idan Kin, Ottawa (CA); Genichi Ohta, Tokyo (JP); Kazuo Teraishi, Tokyo (JP); Kiyoshi Watanabe, Tokyo (JP) (Continued) (73) Assignee: Zeon Corporation, Tokyo (JP) FOREIGN PATENT DOCUMENTS (*) Notice: Subject to any disclaimer, the term of this EP 587434 A1 3, 1994 patent is extended or adjusted under 35 U.S.C. 154(b) by 349 days. (Continued) (21) Appl. No.: 10/481,340 OTHER PUBLICATIONS (22) PCT Filed: Jun. 27, 2002 Edited by Kagaku Daijiten Henshu Iinkai, “Kagaku Daijiten 9”. (86). PCT No.: PCT/UP02/06501 Kyoritsu Shuppan Co., Ltd., Aug. 25, 1962, p. 437, "Yozai'. (Continued) S371 (c)(1), (2), (4) Date: Sep. 24, 2004 Primary Examiner Gregory E Webb (74) Attorney, Agent, or Firm—Birch, Stewart, Kolasch & (87) PCT Pub. No.: WO03/002500 Birch, LLP PCT Pub. Date: Jan. 9, 2003 (57) ABSTRACT (65) Prior Publication Data The present inventions are (A) a solvent comprising at least US 2005/OO65060A1 Mar. 24, 2005 one cycloalkyl alkyl ether (1) represented by the general O O formula: R1-O R2 (wherein R1 is cyclopentyl or the like: (30) Foreign Application Priority Data and R2 is C1-10 alkyl or the like); (B) a method of prepara Jun. 28, 2001 (JP) ............................. 2001-196766 tions the ethers (1) characterized by reacting an alicyclic Oct.
    [Show full text]
  • Syntheses and Eliminations of Cyclopentyl Derivatives David John Rausch Iowa State University
    Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1966 Syntheses and eliminations of cyclopentyl derivatives David John Rausch Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Rausch, David John, "Syntheses and eliminations of cyclopentyl derivatives " (1966). Retrospective Theses and Dissertations. 2875. https://lib.dr.iastate.edu/rtd/2875 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. This dissertation has been microfilmed exactly as received 66—6996 RAUSCH, David John, 1940- SYNTHESES AND ELIMINATIONS OF CYCLOPENTYL DERIVATIVES. Iowa State University of Science and Technology Ph.D., 1966 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan SYNTHESES AND ELIMINATIONS OF CYCLOPENTYL DERIVATIVES by David John Rausch A Dissertation Submitted to the Graduate Faculty in Partial Fulfillment of The Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Subject: Organic Chemistry Approved : Signature was redacted for privacy. Signature was redacted for privacy. Head of Major Department Signature was redacted for privacy. Iowa State University Of Science and Technology Ames, Iowa 1966 ii TABLE OF CONTENTS VITA INTRODUCTION HISTORICAL Conformation of Cyclopentanes Elimination Reactions RESULTS AND DISCUSSION Synthetic Elimination Reactions EXPERIMENTAL Preparation and Purification of Materials Procedures and Data for Beta Elimination Reactions SUMMARY LITERATURE CITED ACKNOWLEDGEMENTS iii VITA The author was born in Aurora, Illinois, on October 24, 1940, to Mr.
    [Show full text]
  • Cyclopentanol. Part I: Quantum Chemistry Calculation and Kinetic Modeling
    Exploring the combustion chemistry of a novel lignocellulose-derived biofuel: cyclopentanol. Part I: quantum chemistry calculation and kinetic modeling Item Type Article Authors Cai, Liming; Kröger, Leif; Döntgen, M.; Leonhard, Kai; Narayanaswamy, Krithika; Sarathy, Mani; Heufer, Karl Alexander; Pitsch, H. Citation Cai, L., Kröger, L., Döntgen, M., Leonhard, K., Narayanaswamy, K., Sarathy, S. M., … Pitsch, H. (2019). Exploring the combustion chemistry of a novel lignocellulose-derived biofuel: cyclopentanol. Part I: quantum chemistry calculation and kinetic modeling. Combustion and Flame, 210, 490–501. doi:10.1016/ j.combustflame.2019.07.012 Eprint version Pre-print DOI 10.1016/j.combustflame.2019.07.012 Publisher Elsevier BV Journal Combustion and Flame Rights NOTICE: this is the author’s version of a work that was accepted for publication in Combustion and Flame. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Combustion and Flame, [[Volume], [Issue], (2019-01-01)] DOI: 10.1016/j.combustflame.2019.07.012 . © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ Download date 29/09/2021 13:28:38 Item License http://creativecommons.org/licenses/by-nc-nd/4.0/ Link to Item http://hdl.handle.net/10754/656743 Exploring the combustion chemistry of a novel lignocellulose-derived biofuel: cyclopentanol. Part I: quantum chemistry calculation and kinetic modeling Liming Caia,∗, Leif Kr¨ogerb, Malte D¨ontgenb, Kai Leonhardb, Krithika Narayanaswamyc, S.
    [Show full text]
  • In Acidic Medium
    Journal of Chemistry and Chemical Sciences, Vol. 5(7), 414-423, July 2015 ISSN 2229-760X (Print) (An International Research Journal), www.chemistry-journal.org ISSN 2319-7625 (Online) Kinetic and Mechanistic Study of Ru (III) Catalyzedoxidation of Galactitol by Chloramine-T: in Acidic medium. Amrita Srivastava and Swarn Lata Bansal Department of Chemistry, University of Lucknow, Lucknow, INDIA. email:[email protected], [email protected]. (Received on: July 29, 2015) ABSTRACT Kinetics and mechanismof Ru (III)-catalysed oxidation ofGalactitolby N- chlorosulphonamide (CAT) have been investigated in perchlorlc acid media in the presence of mercuric acetate as chloride ion scavenger. The results showed zero order kinetics with respect to galactitol and first order with respect to Ru (lll) and chloramine-T. There is no effect of sodium perchlorate, KCl and mercuric acetate show zero effect on reaction rate. Various activation parameters have been computed. Galatonic acid has been identified as the products, and a suitable mechanism consistent with observed kinetic results has been proposed. Keywords: Kinetics, oxidation, galactitol, chloramine-T, Ru (III) catalyst, mercuric acetate. INTRODUCTION Sugar alcohols are obtained through hydrogenation of mono- and disaccharides. The most common sugar alcohols derived from monosaccharaides are sorbitol, mannitol, erythritol, xylitol and galactitol. Most of these sugar alcohols are chemically converted from corresponding sugars using a metal catalyst such as raney-nickel. Galactitol (Dulcitol) is a naturally occurring sugar alcohol with six carbon atoms, the reduction product of galactose. It is a saccharine substances (C 6H14 O6) and isomeric with mannitol. In the people with galactokinase deficiency is a form in the lens of eye leading to cataracts.
    [Show full text]
  • Rate and Product Studies on the Oxidative Cleavage of Some Bicyclic Alcohols with Ceric Ammonium Nitrate Patrick John Flash Iowa State University
    Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1970 Rate and product studies on the oxidative cleavage of some bicyclic alcohols with ceric ammonium nitrate Patrick John Flash Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Flash, Patrick John, "Rate and product studies on the oxidative cleavage of some bicyclic alcohols with ceric ammonium nitrate " (1970). Retrospective Theses and Dissertations. 4306. https://lib.dr.iastate.edu/rtd/4306 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. 71-7267 FLASH, Patrick John, 1942- RATE AND PRODUCT STUDIES ON THE OXIDATIVE CLEAVAGE OF SOME BICYCLIC ALCOHOLS WITH CERIC AMMONIUM NITRATE. Iowa State University, Ph.D., 1970 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan THIS DISSERTATION HAS BEEN MICROFILMED EXACTLY AS RECEIVED RATE AND PRODUCT STUDIES ON THE OXIDATIVE CLEAVAGE OF SOME BICYCLIC ALCOHOLS WITH CERIC AMMONIUM NITRATE by Patrick John Flash A Dissertation Submitted to the Graduate Faculty in Partial Fulfillment of The Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Subject: Organic
    [Show full text]
  • Tribological Performance of Biomass-Derived Bio-Alcohol and Bio-Ketone Fuels
    energies Article Tribological Performance of Biomass-Derived Bio-Alcohol and Bio-Ketone Fuels Omid Doustdar , Soheil Zeraati-Rezaei, Jose Martin Herreros , Athanasios Tsolakis *, Karl D. Dearn and Miroslaw Lech Wyszynski Department of Mechanical Engineering, School of Engineering, University of Birmingham, Birmingham B15 2TT, UK; [email protected] (O.D.); [email protected] (S.Z.-R.); [email protected] (J.M.H.); [email protected] (K.D.D.); [email protected] (M.L.W.) * Correspondence: [email protected] Abstract: This study relates to developing future alternative fuels and focuses on the effects of a fuel’s molecular structure on its properties and performance in advanced propulsion systems. The tribological performance of various biomass-derived oxygenated alternative fuels, including butanol, pentanol, cyclopentanol, cyclopentanone, and gasoline and their blends with diesel, was investigated. Lubricity tests were conducted using a high-frequency reciprocating rig (HFRR). Cyclopentanone-diesel and cyclopentanol-diesel blends result in smaller wear scar sizes compared to using their neat forms. A lower steel disc contaminated with the alternative fuels during the HFRR tests resulted in worn surface roughness values lower than those of the neat diesel by up to 20%. It is believed that these reductions are mainly due to the presence of the hydroxyl group and the carbonyl group in alcohols and ketones, respectively, which make them more polar and consequently helps the formation of the protective lubrication film on the worn moving surfaces during the sliding Citation: Doustdar, O.; Zeraati- process. Overall, the results from this study indicate that environmentally friendly cyclopentanol and Rezaei, S.; Herreros, J.M.; Tsolakis, A.; cyclopentanone are practical and efficient fuel candidates for future advanced propulsion systems.
    [Show full text]
  • Dielectric Constant Chart
    Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG. F CONSTANT ABS RESIN, LUMP 2.4-4.1 ABS RESIN, PELLET 1.5-2.5 ACENAPHTHENE 70 3 ACETAL 70 3.6 ACETAL BROMIDE 16.5 ACETAL DOXIME 68 3.4 ACETALDEHYDE 41 21.8 ACETAMIDE 68 4 ACETAMIDE 180 59 ACETAMIDE 41 ACETANILIDE 71 2.9 ACETIC ACID 68 6.2 ACETIC ACID (36 DEGREES F) 36 4.1 ACETIC ANHYDRIDE 66 21 ACETONE 77 20.7 ACETONE 127 17.7 ACETONE 32 1.0159 ACETONITRILE 70 37.5 ACETOPHENONE 75 17.3 ACETOXIME 24 3 ACETYL ACETONE 68 23.1 ACETYL BROMIDE 68 16.5 ACETYL CHLORIDE 68 15.8 ACETYLE ACETONE 68 25 ACETYLENE 32 1.0217 ACETYLMETHYL HEXYL KETONE 66 27.9 ACRYLIC RESIN 2.7 - 4.5 ACTEAL 21 3.6 ACTETAMIDE 4 AIR 1 AIR (DRY) 68 1.000536 ALCOHOL, INDUSTRIAL 16-31 ALKYD RESIN 3.5-5 ALLYL ALCOHOL 58 22 ALLYL BROMIDE 66 7 ALLYL CHLORIDE 68 8.2 ALLYL IODIDE 66 6.1 ALLYL ISOTHIOCYANATE 64 17.2 ALLYL RESIN (CAST) 3.6 - 4.5 ALUMINA 9.3-11.5 ALUMINA 4.5 ALUMINA CHINA 3.1-3.9 ALUMINUM BROMIDE 212 3.4 ALUMINUM FLUORIDE 2.2 ALUMINUM HYDROXIDE 2.2 ALUMINUM OLEATE 68 2.4 1 Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG. F CONSTANT ALUMINUM PHOSPHATE 6 ALUMINUM POWDER 1.6-1.8 AMBER 2.8-2.9 AMINOALKYD RESIN 3.9-4.2 AMMONIA -74 25 AMMONIA -30 22 AMMONIA 40 18.9 AMMONIA 69 16.5 AMMONIA (GAS?) 32 1.0072 AMMONIUM BROMIDE 7.2 AMMONIUM CHLORIDE 7 AMYL ACETATE 68 5 AMYL ALCOHOL -180 35.5 AMYL ALCOHOL 68 15.8 AMYL ALCOHOL 140 11.2 AMYL BENZOATE 68 5.1 AMYL BROMIDE 50 6.3 AMYL CHLORIDE 52 6.6 AMYL ETHER 60 3.1 AMYL FORMATE 66 5.7 AMYL IODIDE 62 6.9 AMYL NITRATE 62 9.1 AMYL THIOCYANATE 68 17.4 AMYLAMINE 72 4.6 AMYLENE 70 2 AMYLENE BROMIDE 58 5.6 AMYLENETETRARARBOXYLATE 66 4.4 AMYLMERCAPTAN 68 4.7 ANILINE 32 7.8 ANILINE 68 7.3 ANILINE 212 5.5 ANILINE FORMALDEHYDE RESIN 3.5 - 3.6 ANILINE RESIN 3.4-3.8 ANISALDEHYDE 68 15.8 ANISALDOXINE 145 9.2 ANISOLE 68 4.3 ANITMONY TRICHLORIDE 5.3 ANTIMONY PENTACHLORIDE 68 3.2 ANTIMONY TRIBROMIDE 212 20.9 ANTIMONY TRICHLORIDE 166 33 ANTIMONY TRICHLORIDE 5.3 ANTIMONY TRICODIDE 347 13.9 APATITE 7.4 2 Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG.
    [Show full text]
  • Atmospheric Chemistry of Alcohols
    J. Braz. Chem. Soc., Vol. 8, No. 4, 433-442, 1997. © 1997 Soc. Bras. Química Printed in Brazil. 0103 – 5053 $6.00 + 0.00 Review Atmospheric Chemistry of Alcohols Daniel Grosjean DGA, Inc., 4526 Telephone Road, Suite 205, Ventura, CA 93003 USA Received: September 7, 1996 A química atmosférica dos álcoois, os quais são largamente empregados como combustíveis de veículos leves (como o etanol no Brasil) e solventes industriais, foi revista com o foco centralizado em seus aspectos de cinética e mecanismos de reação. A oxidação dos álcoois na atmosfera envolve sua reação com radicais hidroxil (OH). São apresentadas constantes de velocidade para a reação álcool-OH de 33 álcoois saturados, incluindo compostos mono e difuncionais. As meias-vidas atmosféricas são, respectivamente, de uma semana para metanol e t-butil álcool, 2,5 dias para etanol, e de 8-15 h para outros álcoois. São descritos estudos de laboratório para os produtos de reações álcool-OH, e mecanismos são assinalados. Os produtos que predominam são o formaldeído para o metanol, acetaldeído para etanol, acetona para 2-propanol, 2-butanona e acetaldeído para o 2-butanol e acetona e formaldeído para o t-butil álcool. A reação de OH com os álcoois envolve a abstração de um átomo de hidrogênio da ligação C-H, ao passo que na ligação O-H esta abstração é negligível. Os radicais alquil (R) e α-hidroxialquil assim formados reagem então com oxigênio. Essa reação envolve adição para os radicais alquil (R + O2 → RO2) e abstração de H dos radicais α-hidroxialquil (ex. etanol + OH → CH3CHOH, CH3CHOH + O2 → HO2 + CH3CHO).
    [Show full text]
  • Catalytic Amidation of Natural and Synthetic Polyol Esters with Sulfonamides
    ARTICLE https://doi.org/10.1038/s41467-019-11864-9 OPEN Catalytic amidation of natural and synthetic polyol esters with sulfonamides Hua Liu1, Yi-Ling Zhu1 & Zhi Li 1 Triacylglycerides are naturally abundant and renewable feedstock for biofuels and chemicals. In this report, these seemingly stable compounds are shown to be reactive toward a variety of sulfonamides under Lewis acid catalysis. In these reactions, alkyl C(sp3)–O bonds are cleaved – 1234567890():,; and C N bonds constructed, providing functionalized value-added products directly from renewables. Mechanistic and scope study demonstrate that the origin of the reactivity could be the synergy of Lewis acid catalysis and neighboring group participation by the 2- or 3-acyloxy or acylamido group with respect to the reactive site. Since poly(ethylene terephthalate) (PET), a widely available consumer polyester, also contains 1,2-diol diester group as the repeating unit in the main chain, this chemistry can also be applied to efficient depolymerization of PET. 1 School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China. Correspondence and requests for materials should be addressed to Z.L. (email: [email protected]) NATURE COMMUNICATIONS | (2019) 10:3881 | https://doi.org/10.1038/s41467-019-11864-9 | www.nature.com/naturecommunications 1 ARTICLE NATURE COMMUNICATIONS | https://doi.org/10.1038/s41467-019-11864-9 iodiesel is an appealing source of renewable energy that mediated conditions, and so do TAGs33. Therefore, Lewis acid- Breceived elevated attention in the recent decades1. Biojetfuel catalyzed formation of acyloxonium intermediates and their blends derived from plant oils reportedly reduced the catalytic hydrogenation could also be one of the operating emission of pollution particles comparing with traditional jet mechanisms in the hydrogenolysis of TAGs.
    [Show full text]
  • Alcohols and Phenols
    Alcohols and Phenols Klein, D. (2012). Alcohols and Phenols. En Organic Chemistry (pp. 564-570). USA: Wiley. Espacio de Formación Multimodal 13 Alcohols and 13.1 Structure and Properties of Alcohols Phenols 13.2 Acidity of Alcohols and Phenols 13.3 Preparation of Alcohols via DID YOU EVER WONDER… Substitution or Addition what causes the hangover associated with 13.4 Preparation of Alcohols via Reduction drinking alcohol and whether anything 13.5 Preparation of Diols can be done to prevent a hangover? 13.6 Preparation of Alcohols via Grignard Reagents 13.7 Protection of Alcohols eisalgia, the medical term for a hangover, refers to the unpleas- 13.8 Preparation of Phenols Vant physiological effects that result from drinking too much 13.9 Reactions of Alcohols: alcohol. These effects include headache, nausea, vomiting, fatigue, Substitution and Elimination and a heightened sensitivity to light and noise. Hangovers are caused 13.10 Reactions of Alcohols: Oxidation by a multitude of factors. These factors include (but 13.11 Biological Redox Reactions are not limited to) dehydration caused by the 13.12 Oxidation of Phenol stimulation of urine production, the loss of 13.13 Synthesis Strategies vitamin B, and the production of acetal- dehyde in the body. Acetaldehyde is a product of the oxidation of ethanol. Oxidation is just one of the many reac- tions that alcohols undergo. In this chapter, we will learn about alcohols and their reactions. Then, we will revisit the topic of acetaldehyde production in the body, and we will see if anything can be done to prevent a hangover. klein_c13_564-621hr.indd 564 11/8/10 2:10 PM 13.1 Structure and Properties of Alcohols 565 DO YOU REMEMBER? Before you go on, be sure you understand the following topics.
    [Show full text]
  • Preparation of 6-Cyclopentyl Derivatives of 2-Naphthalenone
    University of Montana ScholarWorks at University of Montana Graduate Student Theses, Dissertations, & Professional Papers Graduate School 1966 Preparation of 6-cyclopentyl derivatives of 2-naphthalenone Bonnie Ann Bukwa The University of Montana Follow this and additional works at: https://scholarworks.umt.edu/etd Let us know how access to this document benefits ou.y Recommended Citation Bukwa, Bonnie Ann, "Preparation of 6-cyclopentyl derivatives of 2-naphthalenone" (1966). Graduate Student Theses, Dissertations, & Professional Papers. 3289. https://scholarworks.umt.edu/etd/3289 This Thesis is brought to you for free and open access by the Graduate School at ScholarWorks at University of Montana. It has been accepted for inclusion in Graduate Student Theses, Dissertations, & Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. THE IREPARATiQN OF é-GYCLOPEHTÏL DERIVATIVES OF 2-NAPHTHAimONE by BONNIE A. BUKWA B.S, Michigan Teehaological University, I964 Presented im partial fulfillment of the requirements for the degree of Master of Science UNIVERSITY OF MONTANA 1966 Approved bys Chairman tS-raduate School 1967 JAN 4 Date UMI Number: EP34656 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent on the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. UMI EP34656 Copyright 2012 by ProQuest LLC. All rights reserved. This edition of the work is protected against unauthorized copying under Title 17, United States Code.
    [Show full text]
  • United States Patent (19) (11) 4,092,315 Bianco 45) May 30, 1978 (54) NOVEL CRYSTALLINE FORMS of PRAZOSN HYDROCHLORDE OTHER PUBLICATIONS Weissberger, A
    United States Patent (19) (11) 4,092,315 Bianco 45) May 30, 1978 (54) NOVEL CRYSTALLINE FORMS OF PRAZOSN HYDROCHLORDE OTHER PUBLICATIONS Weissberger, A. Ed., "Technique of Organic Chem.", (75) Inventor: Ernest J. Bianco, Niantic, Conn. vol. III, Interscience N.Y., N.Y., (1950). 73 Assignee: Pfizer Inc., New York, N.Y. Primary Examiner-Alton D. Rollins Assistant Examiner-D. B. Springer (21) Appl. No.: 662,937 Attorney, Agent, or Firm-Connolly and Hutz 22 Filed: Mar. 1, 1976 57 ABSTRACT The invention relates to novel and valuable crystalline 51) Int. C.’............................................ CO7D 239/94 forms of the hypotensive agent prazosin hydrochloride. 52 U.S. C. .................................... 544/291; 424/251 The anhydrous a-form is preferred because it is rela 58 Field of Search .................. 260/256.4 Q; 424/251 tively non-hygroscopic and hence possesses important (56) References Cited advantages in handling and formulation. The polyhy drate form of prazosin hydrochloride is preferred be U.S. PATENT DOCUMENTS cause of its low, uniform rate of dissolution. 3,635,979 1/1972 Hess .............................. 260/256.4 Q 3,663,706 5/1972 Hess ..................................... 424/251 4 Claims, 6 Drawing Figures U.S. Patent May 30, 1978 Sheet 1 of 6 4,092,315 IIT III IIST s S s T TNs. - SETIN. S.22s) & ITIL || sTSS-1c S st | | | || || TST II SST Hills STT N SN ERT IIIs TTSEE N N O | | | | | | ls. E.e s SS C R55 s TTTFIIs S. TT SI ITT cy S || || || NIIT II ST N & NIT S-3se a Wy Y NT TTTM les SS S N S S S S & S (2a1a2.2, asaraut U.
    [Show full text]